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Gmp Data Reviewer Jobs (NOW HIRING)

Thermo Fisher

Data Reviewer - Microbiology

Previous experience with formal data review in GMP Lab strongly preferred * Previous experience in microbiological testing environments preferred * To demonstrate behaviors which align to the 4i ...

New

CEDENT

Data Reviewer, Quality Control

Verona, WI

The Data Reviewer is responsible for ensuring the completion, quality, and compliance of laboratory ... GMP) standards. This position will manage deadlines for review completion and aid in the ...

Eurofins

QC Data Reviewer - LNP and Lipids

Boston, MA · On-site

The role requires attention to detail, familiarity with GMP practices, and the ability to ensure data integrity and regulatory compliance. * Review analytical data packages from stability studies ...

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How much do gmp data reviewer jobs pay per hour?

As of Jun 29, 2026, the average hourly pay for gmp data reviewer in the United States is $26.24, according to ZipRecruiter salary data. Most workers in this role earn between $14.42 and $36.30 per hour, depending on experience, location, and employer.

What are some common challenges faced by GMP Data Reviewers during the documentation review process?

GMP Data Reviewers often encounter challenges such as inconsistent data entries, incomplete documentation, and discrepancies that require clarification with laboratory or production staff. Managing tight deadlines while ensuring compliance with regulatory standards can also be demanding. Effective communication with cross-functional teams is essential for resolving issues quickly and maintaining data integrity, making attention to detail and strong organizational skills crucial for success in this role.

What are the key skills and qualifications needed to thrive as a GMP Data Reviewer, and why are they important?

To thrive as a GMP Data Reviewer, you need a solid understanding of Good Manufacturing Practices, analytical techniques, and a relevant science degree or equivalent experience. Familiarity with laboratory information management systems (LIMS), chromatography data systems, and knowledge of regulatory documentation standards is essential. Attention to detail, critical thinking, and effective communication are vital soft skills for identifying discrepancies and ensuring compliance. These competencies are crucial to maintain data integrity and regulatory compliance in pharmaceutical manufacturing processes.

What are GMP Data Reviewers?

GMP Data Reviewers are professionals responsible for reviewing and verifying data generated in Good Manufacturing Practice (GMP) environments, typically within the pharmaceutical, biotechnology, or medical device industries. Their main role is to ensure that all laboratory and manufacturing records comply with regulatory and quality standards, such as those set by the FDA or EMA. They meticulously check documentation for accuracy, completeness, and adherence to protocols to support product quality and regulatory compliance. GMP Data Reviewers often collaborate with laboratory analysts, quality assurance teams, and regulatory affairs to resolve discrepancies and maintain data integrity.
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Gmp Data Reviewer jobs near you
Infographic showing various Gmp Data Reviewer job openings in the United States as of June 2026, with employment types broken down into 17% As Needed, 33% Full Time, and 50% Contract. Highlights an 87% Physical, 3% Hybrid, and 10% Remote job distribution, with an average salary of $54,583 per year, or $26.2 per hour.
GMP Data Reviewers, Chemists, Metrology Positions

GMP Data Reviewers, Chemists, Metrology Positions

Quality Chemical Laboratories

Wilmington, NC

Full-time

Posted 7 days ago

Job description

GMP Data Reviewers, Chemists, Metrology, LabWare, CPU Validation, Stability, Sample Log-In, and Document Control Positions

Quality Chemical Laboratories (QCL), a pharmaceutical testing and development lab in Wilmington, is seeking highly motivated candidates for qualified analytical data reviewers, LabWare LIMS development/configuration/validation, Document Control Associates, Computer System Validation and Data Integrity Specialists, Scientists (all levels) with experience in Mass Spec, LC, GC, QC compendial testing, Wet Chemistry, Microbiology, Sterility, Synthetic Chemistry, Pharmaceutical Formulation (with knowledge of manufacturing equipment), Metrology, and Sample Log-In Associates.

Special attention is given to candidates with an advanced degree in Chemistry or related science and experience in method development/validation. Special consideration will also be given to experienced GMP data reviewers.

Quality Chemical Laboratories (QCL) is a rapidly growing pharmaceutical testing and manufacturing lab in Wilmington, NC. We are seeking highly motivated candidates for multiple positions throughout the company in the areas of analytical data review, LabWare LIMS development/configuration/validation, Document Control, Computer System Validation and Data Integrity Specialists, Scientists (all levels) with experience in Mass Spec, LC, GC, QC compendial testing, Wet Chemistry, Microbiology, Sterility, Synthetic Chemistry, Biotech, Pharmaceutical Formulation and Manufacturing (requires knowledge of manufacturing equipment), Validation Engineers, Metrology, Report Generation, Sample Log-In Associates, and HVAC Technicians. Special attention given to candidates with an advanced degree in Chemistry or related science and experience in method development/validation. Special consideration also given to experienced GMP data reviewers.

QCL offers competitive salaries commensurate with experience and an excellent benefits package, as well as great potential for career advancement and leadership in a rapidly growing company. We now also offer subsidized childcare at our newly acquired childcare facility.

QCL is an equal opportunity employer.


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